Colon Cancer: Gene >> RAB3GAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264158
Start	135052457:135052457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141518860
CDS Mutation	c.46G>A
AA Mutation	p.Asp16Asn(p.D16N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264158
Start	135162808:135162808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2447G>A
AA Mutation	p.Ser816Asn(p.S816N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264158
Start	135162603:135162603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2338C>A
AA Mutation	p.Leu780Met(p.L780M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264158
Start	135164667:135164667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2680A>T
AA Mutation	p.Ile894Phe(p.I894F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264158
Start	135115293:135115293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.560G>A
AA Mutation	p.Arg187Gln(p.R187Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264158
Start	135113212:135113212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766549363
CDS Mutation	c.424G>A
AA Mutation	p.Glu142Lys(p.E142K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264158
Start	135126605:135126605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.922C>T
AA Mutation	p.Pro308Ser(p.P308S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264158
Start	135113169:135113169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778655079
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264158
Start	135132906:135132906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1248T>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RAB3GAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264158
Start	135126608:135126608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.925C>T
AA Mutation	p.His309Tyr(p.H309Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264158
Start	135093637:135093637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.306A>C
AA Mutation	p.Gln102His(p.Q102H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264158
Start	135115320:135115320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587G>T
AA Mutation	p.Arg196Ile(p.R196I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264158
Start	135130680:135130680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1195G>A
AA Mutation	p.Glu399Lys(p.E399K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264158
Start	135132921:135132921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1263G>T
AA Mutation	p.Glu421Asp(p.E421D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript